[go: up one dir, main page]

BRPI9907084B8 - processo para a preparação de uma composição compreendendo cefalosporina amorfa cristalograficamente estável - Google Patents

processo para a preparação de uma composição compreendendo cefalosporina amorfa cristalograficamente estável

Info

Publication number
BRPI9907084B8
BRPI9907084B8 BRPI9907084A BR9907084A BRPI9907084B8 BR PI9907084 B8 BRPI9907084 B8 BR PI9907084B8 BR PI9907084 A BRPI9907084 A BR PI9907084A BR 9907084 A BR9907084 A BR 9907084A BR PI9907084 B8 BRPI9907084 B8 BR PI9907084B8
Authority
BR
Brazil
Prior art keywords
preparing
product
composition
high molecular
water
Prior art date
Application number
BRPI9907084A
Other languages
English (en)
Portuguese (pt)
Other versions
BR9907084A (pt
BRPI9907084B1 (pt
Inventor
Iinuma Katsuharu
Yasui Kiyoshi
Onodera Masahiro
Sukegawa Masamichi
Watanabe Tatsuo
Sato Toyomi
Murai Yasushi
Original Assignee
Meiji Seika Kaisha
Meiji Seika Pharma Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Meiji Seika Kaisha, Meiji Seika Pharma Co Ltd filed Critical Meiji Seika Kaisha
Publication of BR9907084A publication Critical patent/BR9907084A/pt
Publication of BRPI9907084B1 publication Critical patent/BRPI9907084B1/pt
Publication of BRPI9907084B8 publication Critical patent/BRPI9907084B8/pt

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/38Cellulose; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • A61K31/546Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Inorganic Chemistry (AREA)
  • Cephalosporin Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
BRPI9907084A 1998-01-07 1999-01-07 processo para a preparação de uma composição compreendendo cefalosporina amorfa cristalograficamente estável BRPI9907084B8 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP192098 1998-01-07
PCT/JP1999/000020 WO1999034832A1 (en) 1998-01-07 1999-01-07 Crystallographically stable amorphous cephalosporin compositions and process for producing the same

Publications (3)

Publication Number Publication Date
BR9907084A BR9907084A (pt) 2000-10-17
BRPI9907084B1 BRPI9907084B1 (pt) 2017-04-25
BRPI9907084B8 true BRPI9907084B8 (pt) 2021-05-25

Family

ID=11515039

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI9907084A BRPI9907084B8 (pt) 1998-01-07 1999-01-07 processo para a preparação de uma composição compreendendo cefalosporina amorfa cristalograficamente estável

Country Status (22)

Country Link
US (2) US6342493B1 (tr)
EP (1) EP1051978B1 (tr)
JP (1) JP3413406B2 (tr)
KR (1) KR100435315B1 (tr)
CN (1) CN1151845C (tr)
AU (1) AU736555B2 (tr)
BR (1) BRPI9907084B8 (tr)
CA (1) CA2316841C (tr)
CZ (1) CZ302082B6 (tr)
EA (1) EA002881B1 (tr)
ES (1) ES2393972T3 (tr)
HU (1) HU230295B1 (tr)
ID (1) ID25469A (tr)
IL (2) IL137004A0 (tr)
NZ (1) NZ505871A (tr)
PL (1) PL194097B1 (tr)
PT (1) PT1051978E (tr)
SK (1) SK286631B6 (tr)
TR (1) TR200001903T2 (tr)
TW (1) TW587946B (tr)
UA (1) UA70311C2 (tr)
WO (1) WO1999034832A1 (tr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA002881B1 (ru) * 1998-01-07 2002-10-31 Мейдзи Сейка Кайся Лтд. Кристаллографически стабильные аморфные цефалоспориновые композиции и способ их получения
PE20010635A1 (es) 1999-10-08 2001-08-15 Smithkline Beecham Corp Inhibidores de fab i utiles para el tratamiento de infecciones bacterianas
DK1560584T3 (da) 2001-04-06 2009-05-18 Affinium Pharm Inc Fab I inhibitorer
ES2389179T3 (es) * 2001-04-26 2012-10-23 Meiji Seika Pharma Co., Ltd. Composición de cefditoren pivoxilo amorfo y procedimiento para producir el mismo
ES2358470T3 (es) * 2002-10-02 2011-05-11 Meiji Seika Kaisha Ltd. Composición medicinal antibacteriana con absorptividad oral mejorada.
DK1575951T3 (da) 2002-12-06 2014-09-15 Debiopharm Int Sa Heterocykliske forbindelser, fremgangsmåder til fremstilling deraf og deres anvendelse i terapi
CA2519429C (en) * 2003-03-17 2013-08-06 Affinium Pharmaceuticals, Inc. Pharmaceutical compositions comprising inhibitors of fab i and further antibiotics
US20070167402A1 (en) * 2003-06-20 2007-07-19 Meiji Seika Kaisha, Ltd. Product of coprecipitation of sparingly soluble substance and water-soluble polymer and process for producing the same
ATE539738T1 (de) 2003-10-08 2012-01-15 Meiji Seika Pharma Co Ltd Nichtkristalline antibakterielle zusammensetzung mit cefditoren-pivoxil
WO2005044824A2 (en) * 2003-11-07 2005-05-19 Ranbaxy Laboratories Limited Processes for the preparation of highly pure 3-(2-substituted vinyl) cephalosporin
JP2005162696A (ja) * 2003-12-04 2005-06-23 Nichiko Pharmaceutical Co Ltd 溶出性に優れたセフジトレンピボキシル製剤
WO2005082330A2 (en) * 2004-02-19 2005-09-09 Ranbaxy Laboratories Limited Co-precipitated amorphous cefditoren pivoxil and dosage forms comprising the same
KR101299399B1 (ko) 2004-06-04 2013-08-22 아피늄 파마슈티컬스, 인크. 치료제, 및 그의 제조 및 사용 방법
US20080069879A1 (en) * 2006-05-02 2008-03-20 Ravishekhar Bhiwgade Stable solid dosage form containing amorphous cefditoren pivoxil and process for preparation thereof
WO2008009122A1 (en) 2006-07-20 2008-01-24 Affinium Pharmaceuticals, Inc. Acrylamide derivatives as fab i inhibitors
WO2008057058A1 (en) * 2006-11-10 2008-05-15 Nobel Ilac Sanayii Ve Ticaret As Oral pharmaceutical compositions
EP2125802A4 (en) 2007-02-16 2014-08-20 Debiopharm Int Sa SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS
CN101560216B (zh) * 2009-05-27 2011-06-15 上海交通大学 头孢妥仑酯的制备方法
US20130143857A1 (en) * 2010-07-23 2013-06-06 Lupin Limited Pharmaceutical compositions of cefditoren pivoxil
CN103209966B (zh) 2010-09-30 2015-06-10 富山化学工业株式会社 6-氟-3-羟基-2-吡嗪甲酰胺的钠盐
SG188662A1 (en) 2010-09-30 2013-05-31 Toyama Chemical Co Ltd Meglumine salt of 6-fluoro-3-hydroxy-2-pyrazine carboxamide
BR122021020778B1 (pt) 2012-06-19 2022-07-12 Debiopharm International Sa Derivados de pró-fármaco de (e)-n-metil-n-((3-metilbenzofuran-2-il) metil)-3-(7-oxo-5,6,7,8-tetraidro- 1, 8- naftirindin-3-il) acrilamida
MX371021B (es) * 2013-08-29 2020-01-13 Cadila Healthcare Ltd Procedimiento para preparar saroglitazar o sus sales farmaceuticamente aceptables.
EP3244879A1 (en) 2015-01-16 2017-11-22 Ögün, Yusuf Toktamis Cefditoren pivoxil compositions with improved stability and production methods thereof
SI3419628T1 (sl) 2016-02-26 2021-03-31 Debiopharm International Sa Zdravilo za zdravljenje infekcij diabetičnega stopala
CN109053768A (zh) * 2018-08-07 2018-12-21 中国医药集团总公司四川抗菌素工业研究所 一种无定型头孢妥仑酯的制备方法
PH12021551922A1 (en) 2019-02-14 2022-05-23 Debiopharm Int Sa Afabicin formulation, method for making the same
UA129222C2 (uk) 2019-06-14 2025-02-12 Дебіофарм Інтернешнл С.А. Лікарський засіб і його застосування для лікування бактеріальних інфекцій, пов'язаних з біоплівкою
CN110251467A (zh) * 2019-06-26 2019-09-20 北京济美堂医药研究有限公司 一种无定形态头孢妥仑匹酯组合物的制备方法
CN112190539B (zh) * 2020-11-10 2021-11-02 深圳立健药业有限公司 一种头孢妥仑匹酯组合物及其应用
CN120732800B (zh) * 2025-08-19 2025-12-02 湖南恒昌医药集团股份有限公司 头孢托仑匹酯缓释片及其制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0678234B2 (ja) * 1988-04-19 1994-10-05 明治製菓株式会社 経口投与用抗菌組成物
JPH05306227A (ja) * 1992-04-27 1993-11-19 Lion Corp 徐放性口腔内疾患治療剤
JP2576927B2 (ja) * 1992-05-15 1997-01-29 ファイザー製薬株式会社 細粒核
JPH06316517A (ja) * 1993-02-22 1994-11-15 Grelan Pharmaceut Co Ltd 放出制御製剤
JPH0717866A (ja) * 1993-06-16 1995-01-20 Meiji Seika Kaisha Ltd 医薬組成物
WO1996019239A1 (en) 1994-12-21 1996-06-27 Yamanouchi Pharmaceutical Co., Ltd. Solid composition with improved solubility and absorbability
AR004014A1 (es) * 1995-10-13 1998-09-30 Meiji Seika Kaisha Una composicion antibacteriana de cefditoren pivoxilo para administracion oral y metodo para obtener dicha composicion
NZ330739A (en) 1996-05-20 1999-06-29 Janssen Pharmaceutica Nv Particulate solid dispersion of itraconazole and a water soluble polymer
KR100441907B1 (ko) 1996-09-20 2004-07-27 메이지 세이까 가부시끼가이샤 세프디토렌 피복실 결정성 물질 및 그 제조방법
EA002881B1 (ru) * 1998-01-07 2002-10-31 Мейдзи Сейка Кайся Лтд. Кристаллографически стабильные аморфные цефалоспориновые композиции и способ их получения

Also Published As

Publication number Publication date
TR200001903T2 (tr) 2000-11-21
HK1035148A1 (en) 2001-11-16
HUP0101272A3 (en) 2002-07-29
CN1151845C (zh) 2004-06-02
BR9907084A (pt) 2000-10-17
AU1784599A (en) 1999-07-26
CZ20002542A3 (cs) 2000-12-13
IL137004A (en) 2008-11-03
SK286631B6 (sk) 2009-02-05
ES2393972T3 (es) 2013-01-03
EP1051978A1 (en) 2000-11-15
EA200000742A1 (ru) 2001-02-26
KR100435315B1 (ko) 2004-06-10
IL137004A0 (en) 2001-06-14
CA2316841A1 (en) 1999-07-15
HUP0101272A2 (hu) 2001-12-28
SK10262000A3 (sk) 2001-01-18
TW587946B (en) 2004-05-21
AU736555B2 (en) 2001-08-02
PT1051978E (pt) 2012-11-20
ES2393972T8 (es) 2013-02-25
CZ302082B6 (cs) 2010-09-29
PL341589A1 (en) 2001-04-23
JP3413406B2 (ja) 2003-06-03
NZ505871A (en) 2002-10-25
US6486149B2 (en) 2002-11-26
CA2316841C (en) 2007-11-20
CN1290177A (zh) 2001-04-04
HU230295B1 (hu) 2015-12-28
WO1999034832A8 (en) 1999-10-28
UA70311C2 (uk) 2004-10-15
ID25469A (id) 2000-10-05
US6342493B1 (en) 2002-01-29
KR20010033961A (ko) 2001-04-25
US20020037322A1 (en) 2002-03-28
WO1999034832A1 (en) 1999-07-15
PL194097B1 (pl) 2007-04-30
EP1051978B1 (en) 2012-08-22
EA002881B1 (ru) 2002-10-31
BRPI9907084B1 (pt) 2017-04-25
EP1051978A4 (en) 2007-05-02

Similar Documents

Publication Publication Date Title
BRPI9907084B8 (pt) processo para a preparação de uma composição compreendendo cefalosporina amorfa cristalograficamente estável
IE39517B1 (en) Double salts of s-adenosyl-l-methhionine
HU9401445D0 (en) Nor-bile-acid derivatives, process for producing them and pharmaceutical compositions containing them
CA2334773A1 (en) Benzothiepine-1,1-dioxide derivatives, method for producing them, medicaments containing these compounds and their use
BR0007781A (pt) Conjugado fisiologicamente ativo, composição, e, processo para a produção de um conjugado de peg-gcsf
LTIP862A (en) Method for preparing amino acid derivatives and pharmaceuthical compositions thereof
BG103945A (en) Derivatives of 4"-substituted-9-deoxo-9a-aza-9a-homoerythromycin a
PT81264B (pt) Processo para a preparacao de solucoes injectaveis estabilizadas de piroxicamo
AP9801378A0 (en) 9-amino-3- keto erythromycin derivatives.
GB2198135B (en) Derivatives of cyclohexane
EP0992509A3 (en) Novel macrolide derivatives
GR3026209T3 (en) Compositions containing quinolone antibiotics and sulfonate of polystyrol.
EP0537492A3 (en) Stable salts of 5,10-methylenetetrahydrofolic acid
AP9801377A0 (en) Tricyclic erythromycin derivatives.
DE3369983D1 (en) Isoquinoline derivatives, process for their preparation, pharmaceutical compositions containing them and their use
IE40957B1 (en) A 4-0- ,d glucopyransyl-2-deoxystreptamine, a process for its preparing, and compositions incorporating it
SE8302979D0 (sv) Piperazine derivatives, their production and pharmaceutical compositions containing them
AU636178B2 (en) 7 (alanylaminothiazol-iminoacetamide) substituted cephalosporin derivatives
HRP20020238A2 (en) 4-benzylaminoquinoline conjugates with bile acid and their heteroanalogues, methods for producing the same, medicaments containing these compounds and their use
IL66473A0 (en) Aminoglycoside derivatives,their production and pharmaceutical compositions containing them
IE56229B1 (en) 2-piperazinyl-or-homopiperazinyl-quinazoline derivatives their production and pharmaceutical compositions containing them
GR3023941T3 (en) Cyclic derivatives of angiopeptin, their preparation and their pharmaceutical compositions.
KR850006543A (ko) 세폰니시드 모노나트륨 염
WO1991001963A3 (en) Use of sebacic acid and derivatives thereof in enteral and parenteral nutrition and pharmaceutical compositions containing said compounds
JPS565412A (en) Pharmaceutical composition

Legal Events

Date Code Title Description
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B15K Others concerning applications: alteration of classification

Free format text: ALTERADA DA INT.CL: A61K 9/14, A61K 31/545, A61K 31/546, C07D 501/00, C07D 501/24

Ipc: A61K 47/38 (2009.01), C07D 501/24 (2009.01)

B09B Patent application refused [chapter 9.2 patent gazette]

Free format text: INDEFERIDO O PEDIDO COM BASE NOS ARTIGOS 8O,13 E 25 DA LPI.

B12B Appeal against refusal [chapter 12.2 patent gazette]
B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B09Y Publication of grant cancelled [chapter 9.1.2 patent gazette]

Free format text: REFERENCIA RPI 2147- CODIGO 9.1

B25F Entry of change of name and/or headquarter and transfer of application, patent and certif. of addition of invention: change of name on requirement

Owner name: MEIJI SEIKA KAISHA, LTD (JP)

Free format text: A FIM DE ATENDER A ALTERACAO DE NOME REQUERIDA ATRAVES DA PETICAO NO 20120104493/RJ, DE 08/11/2012, E NECESSARIO APRESENTAR O DOCUMENTO DE ALTERACAO DE NOME NOTARIZADO E COM A DEVIDA LEGALIZACAO CONSULAR.

B25F Entry of change of name and/or headquarter and transfer of application, patent and certif. of addition of invention: change of name on requirement

Owner name: MEIJI SEIKA KAISHA, LTD (JP)

Free format text: A FIM DE ATENDER A ALTERACAO DE NOME REQUERIDA ATRAVES DA PETICAO NO 20130077706/RJ DE 23/09/2013, E NECESSARIO APRESENTAR O DOCUMENTO DE ALTERACAO NOTARIZADO E COM A DEVIDA LEGALIZACAO CONSULAR.

B25E Requested change of name of applicant rejected

Owner name: MEIJI SEIKA KAISHA, LTD (JP)

Free format text: INDEFERIDO(S) O(S) PEDIDO(S) DE ALTERACAO(OES) DE NOME CONTIDO(S) NA PETICAO NO 20120104493, DE 08/11/2012, POR AUSENCIA DE CUMPRIMENTO DA EXIGENCIA PUBLICADA NA RPI NO 2291, DE 02/12/2014.

B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]
B25D Requested change of name of applicant approved
B16C Correction of notification of the grant [chapter 16.3 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 07/01/1999 OBSERVADAS AS CONDICOES LEGAIS. PATENTE CONCEDIDA CONFORME ADI 5.529/DF

B21A Patent or certificate of addition expired [chapter 21.1 patent gazette]

Free format text: PATENTE EXTINTA EM 07/01/2019